Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1241321
rs1241321
Entrez Id: 23576
Gene Symbol: DDAH1
DDAH1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 GeneticVariation BEFREE Our results provide the first evidence that SNP rs1241321 in DDAH1 is associated with type 2 diabetes and its long-term outcome. 21303562 2011
dbSNP: rs3753793
rs3753793
Entrez Id: 3491;23576
Gene Symbol: CCN1;DDAH1
CCN1;DDAH1
CUI: C0018213
Disease:
Graves Disease 		0.010 GeneticVariation BEFREE SNPs rs12136280 (odds ratio [OR] 1.29, p=0.002), rs6663606 (OR 1.26, p=0.004), and rs17534202 (OR 1.21, p=0.02) in BTG2 and rs3753793 (OR 1.21, p=0.03) in CYR61 were associated with GD. 24780075 2014
dbSNP: rs480414
rs480414
Entrez Id: 23576
Gene Symbol: DDAH1
DDAH1
CUI: C0020538
Disease:
Hypertensive disease 		0.010 GeneticVariation BEFREE The frequency of single nucleotide polymorphisms in arginase-1 (ARG1 rs2781666) and dimethylarginine dimethylaminohydrolase-1 (DDAH1 rs480414) genes has been found to differ in a cohort of bronchopulmonary dysplasia patients with pulmonary hypertension (cases) and without pulmonary hypertension (controls). 30267614 2018